Ursolic Acid Triggers Apoptosis in Human Osteosarcoma Cells via Caspase Activation and the ERK1/2 MAPK Pathway

细胞凋亡 夏普 熊果酸 生存素 MAPK/ERK通路 p38丝裂原活化蛋白激酶 细胞生物学 化学 半胱氨酸蛋白酶 激酶 蛋白激酶A 聚ADP核糖聚合酶 分子生物学 生物 生物化学 程序性细胞死亡 聚合酶 色谱法
作者
Chia‐Chieh Wu,Chun-Hsiang Cheng,Yi‐Hui Lee,Ing‐Lin Chang,Hsin-Yao Chen,Chen-Pu Hsieh,Pin Ju Chueh
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:64 (21): 4220-4226 被引量:38
标识
DOI:10.1021/acs.jafc.6b00542
摘要

Ursolic acid (UA), a naturally occurring pentacyclic triterpene acid found in many medicinal herbs and edible plants, has been shown to trigger apoptosis in several lines of tumor cells in vitro. We found that treatment with UA suppressed the viability of human osteosarcoma MG-63 cells and induced cell cycle arrest at sub-G1 and G2/M phases. Furthermore, exposure to UA induced intracellular oxidative stress and collapse of mitochondrial membrane permeability, resulting in the subsequent activation of apoptotic caspases 8, 9, and 3 as well as PARP cleavage, and ultimately apoptosis in MG-63 cells. Moreover, protein analysis of mitogen-activated protein kinase (MAPK)-related protein expression showed an increase in activated ERK1/2, JNK, and p38 MAPK in UA-treated MG-63 cells. In addition, UA-induced apoptosis was significantly abolished in MG-63 cells that had been pretreated with inhibitors of caspase 3, 8, and 9 and ERK1/2. Furthermore, UA-treated MG-63 cells also exhibited an enhancement in Bax/Bcl-2 ratio, whereas anti-apoptotic XIAP and survivin were down-regulated. Taken together, we provide evidence demonstrating that UA mediates caspase-dependent and ERK1/2 MAPK-associated apoptosis in osteosarcoma MG-63 cells.

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